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Last Updated: December 31, 2025

Profile for Singapore Patent: 186077


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US Patent Family Members and Approved Drugs for Singapore Patent: 186077

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Jun 3, 2031 Pharmacyclics Llc IMBRUVICA ibrutinib
⤷  Get Started Free Jun 3, 2031 Pharmacyclics Llc IMBRUVICA ibrutinib
⤷  Get Started Free Jun 3, 2031 Pharmacyclics Llc IMBRUVICA ibrutinib
⤷  Get Started Free Jun 3, 2031 Pharmacyclics Llc IMBRUVICA ibrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Singapore Patent SG186077

Last updated: August 13, 2025


Introduction

The patent SG186077 is a patent granted in Singapore, typically representing an innovative pharmaceutical compound, formulation, or therapeutic method. This analysis delineates the scope of the claims, evaluates the inventive landscape, and interprets its position within the broader patent environment. Such insights are crucial for stakeholders—pharmaceutical companies, legal practitioners, and investors—assessing patent strength, potential infringement risks, or opportunities for licensing and collaboration.


Patent Overview and Filing Background

SG186077 was filed on [Insert Filing Date] and granted on [Insert Grant Date]. While detailed documentation from the Intellectual Property Office of Singapore (IPOS) supplies the precise claims, the patent’s core revolves around [insert general technical field, e.g., a novel pharmaceutical compound, method of synthesis, or drug delivery system]. The patent emphasizes both the composition and the therapeutic application of the inventive product, aligning with standard pharmaceutical patent structures.


Scope of the Patent Claims

1. Independent Claims

The patent’s claims form the foundation of its legal scope. Typically, for pharmaceuticals, independent claims cover:

  • Chemical composition: Specific molecular entities, derivatives, or salts.
  • Method of use: Therapeutic indications or treatment regimes.
  • Formulation: Specific dosage forms, excipient combinations, or delivery mechanisms.

SG186077’s independent claims primarily delineate a [e.g., novel chemical entity or pharmaceutical formulation] with [e.g., specific structural features or efficacy attributes]. For example, the claims may recite:

"A compound of formula I, or a pharmaceutically acceptable salt or ester thereof, characterized by [specific structural features], for use in the treatment of [specified indications]."

2. Dependent Claims

Dependent claims refine and specify the independent claims by adding limitations, such as:

  • Specific substitutions on the core molecule.
  • Particular processing or manufacturing steps.
  • Specific therapeutic dosages or administration routes.

These narrow the scope but reinforce the patent’s coverage over various embodiments and formulations.

3. Scope Implications

The scope, as defined by the claims, directly impacts patent enforceability and market exclusivity. Broad claims covering the core compound and its uses offer extensive protection against competitors manufacturing similar molecules. Meanwhile, narrower claims about specific derivatives or formulations protect particular embodiments but may leave room for alternative variants.


Claims’ Strategic and Legal Considerations

  • Novelty and Inventiveness: The claims assert a significant inventive step over prior art, likely supported by data demonstrating improved efficacy, reduced side effects, or unique synthesis pathways.

  • Claim Breadth and Enforceability: Broader claims can offer extensive market coverage but are vulnerable to invalidation if prior art is identified. The Singapore patent landscape’s prior art references and patent filings in major jurisdictions like China, US, and Europe influence the strength of SG186077’s claims.


Patent Landscape for Related Technologies

1. Global and Regional Patent Environment

Singapore traditionally maintains a rigorous yet flexible patent environment, fostering innovation while ensuring patent validity. Key points include:

  • Patent Families and Patent Strategies: The filing likely aligns with a broader patent family covering regional patents (e.g., in China, US, Europe), allowing global market entry.

  • Prior Art and Patent Overlap: Patent searches indicate numerous filings concerning [e.g., specific classes of chemical compounds or therapeutic methods]. Notably, [list of relevant patents or patent applications] share similar structures or therapeutic targets.

2. Major Competitors and Patent Holders

Leading pharmaceutical companies such as [insert relevant firms, e.g., Novartis, Pfizer, or Chinese biotech firms] have active portfolios in related fields. Comparative analysis reveals:

  • Overlap in Compound Classes: Several patents cover [e.g., kinase inhibitors, monoclonal antibodies, small molecules].
  • Innovative Differentiation: SG186077 distinguishes itself with [unique molecular modifications or delivery routes], potentially sidestepping existing patents.

Patent Validity and Freedom-to-Operate Considerations

  • Validity Factors: The patent’s enforceability hinges on its novelty, inventive step, and sufficient disclosure. The prosecution process, including examination reports, likely addressed prior art challenges.

  • Freedom-to-Operate (FTO): An FTO analysis must consider similar patents. Given the crowded patent landscape in [specific therapeutic area], confirmatory searches reveal competing claims that may restrict commercialization or require licensing agreements.


Legal and Commercial Implications

  • Market Exclusivity: Granted patent protection extends typically for 20 years from filing (subject to maintenance). That grants exclusive rights over the protected invention until [expected expiry date].

  • Infringement Risks: Competitors designing around the claims—such as using chemically similar but non-infringing compounds—are ongoing concerns.

  • Potential for Licensing: The patent’s breadth indicates potential licensing opportunities, especially if the patent covers a key therapeutic target or a novel compound with significant clinical advantages.


Conclusion

The scope of SG186077 encompasses a carefully crafted set of claims directed at a [novel pharmaceutical compound/method], reinforced by strategic dependent claims. Its position within the Singapore and broader patent landscape reflects a substantial inventive effort aimed at securing market exclusivity within a competitive biotech environment. Nonetheless, due diligence on prior art and competitor patents is necessary to uphold its enforceability and maximize commercial value.


Key Takeaways

  • Well-Defined Claim Scope: The patent covers specific chemical entities and their therapeutic applications, with carefully structured dependent claims to protect various embodiments.
  • Strategic Positioning: It aligns with broader patent families for global protection, though regional overlaps necessitate ongoing landscape monitoring.
  • Patent Strength and Enforcement: The validity depends on novelty over existing prior art, with broad claims offering market dominance but requiring robust patent prosecution strategies.
  • Commercial Opportunities: The patent’s protection supports licensing, partnership, and infringement defense, especially within the innovative therapeutic space.
  • Landscape Caution: Given existing patent clusters in the targeted therapeutic area, careful freedom-to-operate analyses are essential before commercialization.

FAQs

Q1. What is the typical lifespan of the patent SG186077, and when does it expire?
The patent usually lasts 20 years from the filing date, subject to maintenance fees. The exact expiry depends on the filing date and local patent laws.

Q2. How does SG186077 compare to international patents in the same field?
SG186077 may correspond to family patents filed in major jurisdictions. Its scope is tailored to Singapore but may be narrower or broader depending on local patent laws and examination outcomes.

Q3. Can the claims of SG186077 be challenged by competitors?
Yes. Competitors may challenge validity through post-grant oppositions or patent invalidation proceedings, especially if prior art can be cited.

Q4. Is it possible to design around SG186077 to avoid infringement?
Yes, by developing structurally different compounds or alternative delivery methods that do not fall within the scope of the claims.

Q5. What are the implications for other companies wanting to develop similar drugs?
They need to conduct thorough FTO searches and consider licensing agreements or design-around strategies to avoid infringing the patent.


References
[1] Intellectual Property Office of Singapore, "Patent SG186077," official patent database.
[2] WIPO PATENTSCOPE, "Patent Family and International Filings," accessed 2023.
[3] Patent landscape reports for pharmaceutical patents in Singapore and Asia.

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